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huahewu1 9.9,25.8,37.3,38.3,51.9,53.7,61.3,63.2,65.6,71.4,79.0,106.5,123.3,124.5,128.1,131.6,137.7,170.9,181.7 Huahewu2 25.2,28.5,32.9,38.7,42.5,45.2,56.7,57.6,57.9,70.8,115.8,121.0,122.9,125.9,128.1,137.2,143.6,154.7,185.5 Huahewu3 18.2,22.8,35.6,38.3,40.7,50.3,54.0,54.2,58.0,61.5,66.1,69.4,72.1,109.2,112.2,121.7,128.0,128.2,131.9,138.6,140.7,179.4 ![]() |
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yyj549: ½ð±Ò+30, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, xiexie 2012-09-10 19:25:38
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yyj549: ½ð±Ò+30, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, xiexie 2012-09-10 19:25:38
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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 9.9,25.8,37.3,38.3,51.9,53.7,61.3,63.2,65.6,71.4,79.0,106.5,123.3,124.5,128.1,131.6,137.7,170.9,181.7 ÈܼÁÑ¡Ï È«²¿ CDCl3 CD3CD2OD CD2Cl2 C5D5N C3D7NO CD3SOCD3 C4D8O (CH3)4Si C4D8O2 CD3COOD C4D8O2 H2O D2O CF3COOD CD3OD ND3 CD3COCD3 C6D6 CD3CN ²éѯ¿ÕÖµ Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½30¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . 14-hydroxy-19-oxogelsenicine C19H20N2O5 ÏàËÆ¶È:78.9% Journal of Natural Products 2006 69 715-718 Isolation of Gelsedine-Type Indole Alkaloids from Gelsemium elegans and Evaluation of the Cytotoxic Activity of Gelsemium Alkaloids for A431 Epidermoid Carcinoma Cells Mariko Kitajima, Tomonori Nakamura, Noriyuki Kogure, Mio Ogawa, Yuka Mitsuno, Kageyoshi Ono, Shingo Yano, Norio Aimi, and Hiromitsu Takayama Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . GS-2 C20H24N2O5 ÏàËÆ¶È:75% Chemical & Pharmaceutical Bulletin 2003 51(10) 1211-1214 New Oxindole Alkaloids and Iridoid from Carolina jasmine (Gelsemium sempervirens AIT. f.) Mariko KITAJIMA, Akiko URANO, Noriyuki KOGURE, Hiromitsu TAKAYAMA, and Norio AIMI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . 14-acetoxygelsenicine C21H25N2O5 ÏàËÆ¶È:71.4% Journal of Natural Products 2006 69 715-718 Isolation of Gelsedine-Type Indole Alkaloids from Gelsemium elegans and Evaluation of the Cytotoxic Activity of Gelsemium Alkaloids for A431 Epidermoid Carcinoma Cells Mariko Kitajima, Tomonori Nakamura, Noriyuki Kogure, Mio Ogawa, Yuka Mitsuno, Kageyoshi Ono, Shingo Yano, Norio Aimi, and Hiromitsu Takayama Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 14,15-dihydroxygelsenicine C19H23N2O5 ÏàËÆ¶È:68.4% Organic Letters 2003 Vol. 5, No. 12 2075-2078 Structure Reinvestigation of Gelsemoxonine, a Constituent of Gelsemium elegans, Reveals a Novel,Azetidine-Containing Indole Alkaloid Mariko Kitajima, Noriyuki Kogure, Kentaro Yamaguchi,Hiromitsu Takayama, and Norio Aimi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 14-acetoxy-15-hydroxygelsenicine C21H24N2O6 ÏàËÆ¶È:66.6% Journal of Natural Products 2006 69 715-718 Isolation of Gelsedine-Type Indole Alkaloids from Gelsemium elegans and Evaluation of the Cytotoxic Activity of Gelsemium Alkaloids for A431 Epidermoid Carcinoma Cells Mariko Kitajima, Tomonori Nakamura, Noriyuki Kogure, Mio Ogawa, Yuka Mitsuno, Kageyoshi Ono, Shingo Yano, Norio Aimi, and Hiromitsu Takayama Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . 14-Hydroxygelsecrotonidine C22H24N2O6 ÏàËÆ¶È:63.6% Tetrahedron 2008 64 7690-7694 Four novel gelsedine-type oxindole alkaloids from Gelsemium elegans Yousuke Yamada, Mariko Kitajima, Noriyuki Kogure, Hiromitsu Takayama Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . Gelselenidine C21H24N2O4 ÏàËÆ¶È:57.1% Tetrahedron 2011 67 4807-4813 Six new monoterpenoid indole alkaloids from the aerial part of Gelsemium elegans Sheng Ouyang, Lei Wang, Qing-Wen Zhang, Guo-Cai Wang, Ying Wang, Xiao-Jun Huang, Xiao-Qi Zhang, Ren-Wang Jiang, Xin-Sheng Yao, Chun-Tao Che, Wen-Cai Ye Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . GS-1 C20H22N2O6 ÏàËÆ¶È:55% Chemical & Pharmaceutical Bulletin 2003 51(10) 1211-1214 New Oxindole Alkaloids and Iridoid from Carolina jasmine (Gelsemium sempervirens AIT. f.) Mariko KITAJIMA, Akiko URANO, Noriyuki KOGURE, Hiromitsu TAKAYAMA, and Norio AIMI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . raucaffrinoline ÏàËÆ¶È:55% Phytochemistry 1980 19 989-991 Structure complete de la raucaffrinoline et filiation avec la vomilenine Francine Libot, Nicole Kunesch, Jacques Poisson Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . compound 9 C20H19N2O7Cl3 ÏàËÆ¶È:55% Tetrahedron 2008 64 7690-7694 Four novel gelsedine-type oxindole alkaloids from Gelsemium elegans Yousuke Yamada, Mariko Kitajima, Noriyuki Kogure, Hiromitsu Takayama Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . Gelsefuranidine C24H25N2O5 ÏàËÆ¶È:54.1% Organic Letters 2006 Vol. 8, No. 14 3085-3088 Four Novel Gelsenicine-Related Oxindole Alkaloids from the Leaves of Gelsemium elegans Benth. Noriyuki Kogure, Naoko Ishii, Mariko Kitajima,Sumphan Wongseripipatana, and Hiromitsu Takayama Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . phomadecalin B C17H22O5 ÏàËÆ¶È:52.6% Journal of Natural Products 2002 65 399-402 Phomadecalins A-D and Phomapentenone A: New Bioactive Metabolites from Phoma sp. NRRL 25697, a Fungal Colonist of Hypoxylon Stromata Yongsheng Che, James B. Gloer, and Donald T. Wicklow Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . Gelsedilam C17H18N2O4 ÏàËÆ¶È:52.6% Organic Letters 2006 Vol. 8, No. 14 3085-3088 Four Novel Gelsenicine-Related Oxindole Alkaloids from the Leaves of Gelsemium elegans Benth. Noriyuki Kogure, Naoko Ishii, Mariko Kitajima,Sumphan Wongseripipatana, and Hiromitsu Takayama Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . Nb-methylgelsedilam C18H20N2O4 ÏàËÆ¶È:52.6% Chemistry ¨C An Asian Journal 2011 6 166-173 Seven New Monoterpenoid Indole Alkaloids from Gelsemium elegans Yousuke Yamada, Mariko Kitajima, Noriyuki Kogure, Sumphan Wongseripipatana, and Hiromitsu Takayama Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . 15-Hydroxy-Nb-methylgelsedilam C18H20N2O5 ÏàËÆ¶È:52.6% Chemistry ¨C An Asian Journal 2011 6 166-173 Seven New Monoterpenoid Indole Alkaloids from Gelsemium elegans Yousuke Yamada, Mariko Kitajima, Noriyuki Kogure, Sumphan Wongseripipatana, and Hiromitsu Takayama Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . 18,19-dehydrocorynoxinic acid C21H24N2O4 ÏàËÆ¶È:52.3% Journal of Natural Products 2008 71(7) 1271-1274 Alkaloids from the Leaves of Uncaria rhynchophylla and Their Inhibitory Activity on NO Production in Lipopolysaccharide-Activated Microglia Dan Yuan, Bin Ma, Chunfu Wu, Jingyu Yang, Lijia Zhang, Suiku Liu, Lijun Wu, and Yoshihiro Kano Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . isorhynchophyllic acid C21H26N2O4 ÏàËÆ¶È:52.3% Chinese Chemical Letters 1992 3 425-426 ISORHYNCHOPHYLLIC ACID,A NEW ALKALOID FROM UNCARLA SINENSIS HONG MEI LIU,XIAO ZHANG FENG,YANG LU AND QI TAI ZHENG Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . gelsevirine ÏàËÆ¶È:52.3% Journal of Natural Products 1986 Vol 49 483 21-Oxogelsevirine, a New Alkaloid from Gelsemium rankinii Yeh Schun, Geoffrey A. Cordell, Mark Garland Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . raucaffrinoline ÏàËÆ¶È:52.3% Phytochemistry 1996 41 969-973 Indole alkaloids from Rauwolfia sellowii Cesar Vicente Ferreira Batista, Jan Schripsema, Robert Verpoorte, Sandra Beatriz Rech, Amelia T. Henriques Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . isorhynchophyllic acid C21H26N2O4 ÏàËÆ¶È:52.3% Phytochemistry 1993 33 707-710 Oxindole alkaloids from Uncaria sinensis Hong-Mei Liu, Xiao-Zhang Feng Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . homopodopetaline ÏàËÆ¶È:52.3% Magnetic Resonance in Chmesitry 2005 43 283-293 NMR study of quinolizidine alkaloids: relative configurations, conformations Phuong Mai Le, Marie-Th¨¦r¨¨se Martin, Nguyen Van Hung, Daniel Gu¨¦nard, Thierry S¨¦venet and Nicole Platzer Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . yohimbinic acid C20H26N2O3 ÏàËÆ¶È:50% Journal of Natural Products 2005 68 848-852 Indole Alkaloids and Other Constituents of Rauwolfia serpentina Atsuko Itoh, Tomoko Kumashiro, Machiko Yamaguchi, Naotaka Nagakura, Yoshiyuki Mizushina, Toyoyuki Nishi, and Takao Tanahashi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . 16-hydroxyalstonal C20H22N2O4 ÏàËÆ¶È:50% Journal of Natural Products 2004 67 547-552 New Indole Alkaloids from Alstonia macrophylla Toh-Seok Kam, and Yeun-Mun Choo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . gelsevirine ÏàËÆ¶È:50% Phytochemistry 1991 30 679-683 Three oxindole alkaloids from Gelsemium species Long-Ze Lin, Schun Yeh, Geoffrey A. Cordell, Chou-Zhou Ni, Jon Clardy Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 25 . compound 7 C20H19N2O6Cl3 ÏàËÆ¶È:50% Organic Letters 2006 Vol. 8, No. 14 3085-3088 Four Novel Gelsenicine-Related Oxindole Alkaloids from the Leaves of Gelsemium elegans Benth. Noriyuki Kogure, Naoko Ishii, Mariko Kitajima,Sumphan Wongseripipatana, and Hiromitsu Takayama Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 26 . Methyl (3S*,3aS*,6aR*,10aR*)-3-benzyloxy-4-methylidene-5-oxoperhydronaphtho[1,8a-c]furan-3-carboxylate C22H26O5 ÏàËÆ¶È:50% Journal of the Chemical Society, Perkin Transactions 1 1996 1523-1529 Chemistry of insect antifeedants from Azadirachta indica(part 21): synthesis of model compounds of azadirachtin using a decalin framework as a functional group scaffolding Mar¨ªa L. de la Puente, Steven V. Ley, Monique S. J. Simmonds and Wally M. Blaney Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 27 . Gelsecrotonidine C22H24N2O5 ÏàËÆ¶È:50% Tetrahedron 2008 64 7690-7694 Four novel gelsedine-type oxindole alkaloids from Gelsemium elegans Yousuke Yamada, Mariko Kitajima, Noriyuki Kogure, Hiromitsu Takayama Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 28 . enamine-carbamate C22H23N2O6Cl3 ÏàËÆ¶È:50% Tetrahedron 2008 64 7690-7694 Four novel gelsedine-type oxindole alkaloids from Gelsemium elegans Yousuke Yamada, Mariko Kitajima, Noriyuki Kogure, Hiromitsu Takayama Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 29 . 14-epi-19R-hydroxypentacycle C23H31N3O3 ÏàËÆ¶È:50% Tetrahedron 1998 54 14845-14858 First total synthesis of 19S-hydroxytacamine, an indole alkaloid from Tabernaemontana eglandulosa, and of its C-19 stereoisomer, 19R-hydroxytacamine Mauri Lounasmaa, David Din Belle, Arto Tolvanen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 30 . cnicin C20H26O7 ÏàËÆ¶È:50% Turkish Journal of Chemistry 1999 23 15-20 Chemical Constituents of Centaurea cuneifolia ÜMİT ASLAN, SEVİL ÖKSÜZ Structure 13C NMR ̼Æ×Ä£Äâͼ |

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¶¹¸ç: ½ð±Ò+4, Ó¦ÖúÖ¸Êý+1, лл 2012-09-10 09:01:28
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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 25.2,28.5,32.9,38.7,42.5,45.2,56.7,57.6,57.9,70.8,115.8,121.0,122.9,125.9,128.1,137.2,143.6,154.7,185.5 ÈܼÁÑ¡Ï È«²¿ CDCl3 CD3CD2OD CD2Cl2 C5D5N C3D7NO CD3SOCD3 C4D8O (CH3)4Si C4D8O2 CD3COOD C4D8O2 H2O D2O CF3COOD CD3OD ND3 CD3COCD3 C6D6 CD3CN ²éѯ¿ÕÖµ Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½46¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . Koumine ÏàËÆ¶È:95% Journal of Natural Products 1989 Vol 52 1180 Structures of (19R)-Kouminol and (19S)-Kouminol from Gelsemium elegans F. Sun, Q. Y. Xing, X. T. Liang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . koumine C20H24N2O2 ÏàËÆ¶È:95% Phytochemistry 1990 29 965-968 19-(R)-and 19-(S)-Hydroxydihydrokoumine from Gelsemium elegans Long-Ze Lin,Geoffrey A. Cordell,Chao-Zhou Ni,Jon Clardy Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . koumine C20H22N2O ÏàËÆ¶È:95% Chinese Traditional and Herbal Drugs 2011 42 222-225 Chemical constituents from Gelsemium elegans ZHANG Zhen, LIU Guang-ming, XIAO Huai, ZHANG Zhen, HE Hong-ping, HAO Xiao-jiang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . (19R)-Kouminol C20H24N2O2 ÏàËÆ¶È:65% Journal of Natural Products 1989 Vol 52 1180 Structures of (19R)-Kouminol and (19S)-Kouminol from Gelsemium elegans F. Sun, Q. Y. Xing, X. T. Liang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . (19S)-Kouminol C20H24N2O2 ÏàËÆ¶È:60% Journal of Natural Products 1989 Vol 52 1180 Structures of (19R)-Kouminol and (19S)-Kouminol from Gelsemium elegans F. Sun, Q. Y. Xing, X. T. Liang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . compound 6 C20H22N2O3 ÏàËÆ¶È:60% Tetrahedron 2004 60 893-900 Isolation, structure elucidation, and total synthesis of two new Chimonanthus alkaloids, chimonamidine and chimonanthidine Hiromitsu Takayama, Yohei Matsuda, Kyohei Masubuchi, Atsushi Ishida, Mariko Kitajima, Norio Aimi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . 2-dehydrogeissoschizoline C19H24N2O ÏàËÆ¶È:57.8% Journal of Natural Products 2002 65 85-88 Indole and ¦Â-Carboline Alkaloids from Geissospermum sericeum Jonathan C. P. Steele, Nigel C. Veitch,Geoffrey C. Kite, Monique S. J. Simmonds,and David C. Warhurst Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . 3-methyl-3-[(E)-octa-2,7-dienyl]-3H-indole C17H21N ÏàËÆ¶È:57.8% Heterocycles 2010 80 779-785 Boron Trichloride Mediated Alkyne-Aldehyde Coupling Reactions Min-Liang Yao, Michael P. Quinn, and George W. Kabalka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . 6,11-dihydro-11-(4-isopropylphenyl)-2,3-dimethoxy[1]benzothiopyrano[2,3-b]indole C26H25NO2S ÏàËÆ¶È:57.8% Heterocycles 2004 63 2785-2795 Preparation of Benzothiopyrano[2,3-b]indoles by the Reaction of 1,3-Dihydroindole-2-thiones with Certain Dienophiles Sukanta Kamila and Ed Biehl* Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . Geissosreticulatine C19H24N2O ÏàËÆ¶È:57.8% Journal of Natural Products 2012 75 928-934 Indole Alkaloids from Geissospermum reticulatum M. Reina, W. Ruiz-Mesia, M. L¨®pez-Rodr¨ªguez, L. Ruiz-Mesia, A. Gonz¨¢lez-Coloma, and R. Mart¨ªnez-D¨ªaz Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . 1-(7,8-Dihydro-8,8-dimethyl-5-p-tolyl-naphthalen-2-yl)-ethan-2-ol C21H24O ÏàËÆ¶È:57.8% Bioorganic & Medicinal Chemistry 2009 17 4345-4359 Retinoid receptor subtype-selective modulators through synthetic modifications of RAR¦Ã agonists Susana Álvarez, Rosana Álvarez, Harshal Khanwalkar, Pierre Germain, G¨¦raldine Lemaire, F¨¢tima Rodr¨ªguez-Barrios, Hinrich Gronemeyer, Ángel R. de Lera Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . natorphine-hydrochloride ÏàËÆ¶È:57.8% Organic Magnetic Resonance 1984 22 258-262 Conformational analogies of morphine agonists and antagonists as revealed by carbon-13 NMR spectroscopy Ernest L. Eliel, Susan Morris-Natschke and Vera M. Kolb Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . 19-(R)-hydroxydihydrokoumine C20H24N2O2 ÏàËÆ¶È:55% Phytochemistry 1990 29 965-968 19-(R)-and 19-(S)-Hydroxydihydrokoumine from Gelsemium elegans Long-Ze Lin,Geoffrey A. Cordell,Chao-Zhou Ni,Jon Clardy Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . 19-(S)-hydroxydihydrokoumine C20H24N2O2 ÏàËÆ¶È:55% Phytochemistry 1990 29 965-968 19-(R)-and 19-(S)-Hydroxydihydrokoumine from Gelsemium elegans Long-Ze Lin,Geoffrey A. Cordell,Chao-Zhou Ni,Jon Clardy Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . vobasenal C20H20O4N ÏàËÆ¶È:55% Phytochemistry 1990 29 3007-3011 Alkaloids from leaves and stem bark of Ervatamia polyneura Pascale Clivio,Bernard Richard,Hamid A. Hadi,Bruno David,Thierry Sevenet,Monique Zeches,Louisette Le Men-Olivier Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . Kounaminal C22H25N3O2 ÏàËÆ¶È:54.5% Chemistry ¨C An Asian Journal 2011 6 166-173 Seven New Monoterpenoid Indole Alkaloids from Gelsemium elegans Yousuke Yamada, Mariko Kitajima, Noriyuki Kogure, Sumphan Wongseripipatana, and Hiromitsu Takayama Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . remijinine C19H24N2O2 ÏàËÆ¶È:52.6% Journal of Natural Products 2004 67 1667-1671 Five New Alkaloids from the Leaves of Remijia peruviana Jess G. Daz, Jos Gavin Sazatornil, Matas Lpez Rodrguez, Lastenia Ruiz Mesa, and Gabriel Vargas Arana Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . cinchonicinol C19H24N2O ÏàËÆ¶È:52.6% Chemical & Pharmaceutical Bulletin 1989 37 358-362 Constituents of the Leaves of Murraya paniculata Collected in Taiwan Fuijo IMAI,Takeshi KINOSHITA and Ushio SANKAWA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . (2,3-Dihydro-1H-inden-1-yl) (2,5-dimethoxyphenyl)methanone ÏàËÆ¶È:52.6% Molecules 2008 13 995-1003 Novel Spiroannulated 3-Benzofuranones. Synthesis and Inhibition of the Human Peptidyl Prolyl cis/trans Isomerase Pin1 Manfred Braun, Anahita Hessamian-Alinejad, Boris F. de Lacroix, Birte H. Alvarez and Gunter Fischer Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . 16-bromomethylestra-1,3,5(10)-triene-3,17-diol 8e C19H25O2Br ÏàËÆ¶È:52.6% Steroids 2006 71 141-153 Neighboring group participation: Part 16. Stereoselective synthesis and receptor-binding examination of the four stereoisomers of 16-bromomethyl-3,17-estradiols Ágota Sz¨¢jli, J¨¢nos Wölfling, Erzs¨¦bet Merny¨¢k, Ren¨¢ta Minorics, Árp¨¢d M¨¢rki, George Falkay, Gyula Schneider Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . l-1-(2,5-dimethoxy-4-methylphenyl)-2-(2-hydroxypropan-2-yl)cyclobutanecarbonitrile C17H23NO3 ÏàËÆ¶È:52.6% Heterocycles 2009 78 1955-1976 Regio and Stereo Selectivity on the ¦Á-Aryl-¦Ä-epoxynitrile Anionic Cyclization Reactions: Modulation towards a 5-Endo or 4-Exo Process Jes¨²s Armando Luj¨¢n-Montelongo, Adri¨¢n V¨¢zquez-S¨¢nchez, and Jos¨¦ Gustavo Ávila-Z¨¢rraga Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . (¡À)-tubifoline C18H22N2 ÏàËÆ¶È:52.6% Heterocycles 2008 75 107-118 A Concise Approach to (¡À)-Tubifoline Based on the Palladium-Catalyzed Cross-Coupling Reaction of Indolylborate Minoru Ishikura, Norinobu Takahashi, Koji Yamada, and Takumi Abe Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . N-{3-[4-(3-aminopropyl)-1-piperazinyl]propyl}-N-thieno[3,4-c]chinolin-4-ylamin C21H29N5S ÏàËÆ¶È:52.6% Pharmazie 2006 61 901-907 Thieno[3,4-c]chinolin-4-yl-amine ¨C Synthese und Pr¨¹fung auf Wirksamkeit gegen Malaria / Thieno[3,4-c]quinoline-4-yl-amines ¨C synthesis and investigation of activity against malaria K. Görlitzer, B. Gabriel, H. Jomaa and J. Wiesner Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . compound 15a C40H36N4O2 ÏàËÆ¶È:52.6% Tetrahedron 2012 68 1595-1605 Rhodium(II) catalyzed intermolecular double C-alkylation: a method for the synthesis of tetraindoles and indolophanes Sengodagounder Muthusamy, Thangaraju Karikalan, Chidambaram Gunanathan, Eringathodi Suresh Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 25 . compound 15b C40H36N4O2 ÏàËÆ¶È:52.6% Tetrahedron 2012 68 1595-1605 Rhodium(II) catalyzed intermolecular double C-alkylation: a method for the synthesis of tetraindoles and indolophanes Sengodagounder Muthusamy, Thangaraju Karikalan, Chidambaram Gunanathan, Eringathodi Suresh Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 26 . compound 7 C20H22N2O4 ÏàËÆ¶È:52.6% Tetrahedron 2004 60 893-900 Isolation, structure elucidation, and total synthesis of two new Chimonanthus alkaloids, chimonamidine and chimonanthidine Hiromitsu Takayama, Yohei Matsuda, Kyohei Masubuchi, Atsushi Ishida, Mariko Kitajima, Norio Aimi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 27 . alpinnanin A ÏàËÆ¶È:52.6% Natural Product Communications 2010 5 1687 - 1708 Naturally Occurring Diarylheptanoids Haining Lv and Gaimei She Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 28 . 3-(2-((ethylamino)methyl)-3H-imidazo[4,5-c]quinolin-3-yl)propan-1-ol C16H20N4O, ÏàËÆ¶È:52.6% Bioorganic & Medicinal Chemistry 2011 19 3801-3811 Preliminary evaluation of a 3H imidazoquinoline library as dual TLR7/TLR8 antagonists Nikunj M. Shukla, Subbalakshmi S. Malladi, Victor Day, Sunil A. David Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 29 . compound 15 C23H29NO4 ÏàËÆ¶È:52.1% Tetrahedron 1998 54 9143-9152 Studies on the synthesis of ¦Â-thevinone derivatives J¨¢nos Marton, Zolt¨¢n Szab¨®, S¨¢ndor Garadnay, Szil¨¢rd Mikl¨®s, S¨¢ndor Makleit Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 30 . (1R,11S,12S,14S,7E,3E)-11,12-epoxycembra-3,7,-15(17)-trien-16,14-olide ÏàËÆ¶È:50% Journal of Natural Products 2006 69 1554-1559 Crassocolides A−F, Cembranoids with a trans-Fused Lactone from the Soft Coral Sarcophyton crassocaule Ho-Cheng Huang, Atallah F. Ahmed, Jui-Hsin Su, Chih-Hua Chao, Yang-Chang Wu, Michael Y. Chiang, and Jyh-Horng Sheu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 31 . 16-hydroxyalstonal C20H22N2O4 ÏàËÆ¶È:50% Journal of Natural Products 2004 67 547-552 New Indole Alkaloids from Alstonia macrophylla Toh-Seok Kam, and Yeun-Mun Choo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 32 . sarcotin L C20H28O2 ÏàËÆ¶È:50% Journal of Natural Products 2002 65 1307-1314 Cytotoxic Pyrrolo- and Furanoterpenoids from the Sponge Sarcotragus Species Yonghong Liu, Jongki Hong, Chong-O. Lee, Kwang Sik Im, Nam Deuk Kim, Jae Sue Choi, and Jee H. Jung Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 33 . acerogenin A methyl ether ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 1983 31 1917-1922 Studies on the Constituents of Aceraceae Plants. IV. Carbon-13 Nuclear Magnetic Resonance Spectra of Acerogenin A, Rhododendrol and Related Compounds, and Structure of Aceroside IV from Acer nikoense MASAYOSHI KUBO,MASAHIRO NAGAI and TAKAO INOUE Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 34 . (3R)(3'-Cyclopentyloxy-4'-methoxy) phenyl-4-aminobutyryl-(S)-(-)-phenyl-ethylamide ÏàËÆ¶È:50% Molecules 1998 3 107-119 Enantiodivergent Synthesis of (R)- and (S)-Rolipram Joachim Demnitz, Luigi LaVecchia, Edmond Bacher, Thomas H. Keller, Thomas M¨¹ller, Friedrich Sch¨¹rch, Hans-Peter Weber and Esteban Pombo-Villar Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 35 . jatrorrhizine ÏàËÆ¶È:50% China Journal of Chinese Materia Medica 2009 34 1097-1100 A new flavonoid glucoside from Huanglian jiedutang decoction MA Zhaotang, YANG Xiuwei, ZHONG Guoyue Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 36 . xestosaprol J C21H20O4 ÏàËÆ¶È:50% Journal of Natural Products 2010 73 1188-1191 Xestosaprols from the Indonesian Marine Sponge Xestospongia sp. Jingqiu Dai, Analia Sorribas, Wesley Y. Yoshida, Michelle Kelly and Philip G. Williams Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 37 . N-desmethoxyhumantenine C20H24N2O2 ÏàËÆ¶È:50% Phytochemistry 1991 30 1311-1315 Oxindole alkaloids from Gelsemium elegans Long-Ze Lin, Geoffrey A. Cordell, Chao-Zhou Ni, Jon Clardy Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 38 . columbamine ÏàËÆ¶È:50% Phytochemistry 1990 29 135-139 Degradation of reticuline in Berberis suspension cultures Stefan Jendrzejewski Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 39 . Fmoc-Val-Ala-¦×(NH-CO-NH)-Leu-OMe C30H40N4O6 ÏàËÆ¶È:50% Indian Journal of Chemistry 2008 47B 910-919 Synthesis of ureidopeptides using pentafluorophenyl carbamates from N¦Á-Fmoc-peptide acids Sureshbabu,Vommina V; Venkataramanarao,Rao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 40 . Fmoc-Leu-Ala-¦×(NH-CO-NH)-Val-OMe C30H40N4O6 ÏàËÆ¶È:50% Indian Journal of Chemistry 2008 47B 910-919 Synthesis of ureidopeptides using pentafluorophenyl carbamates from N¦Á-Fmoc-peptide acids Sureshbabu,Vommina V; Venkataramanarao,Rao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 41 . jatrorrhizine ÏàËÆ¶È:50% Chinese Traditional and Herbal Drugs 2003 34 980-981 ¿í°úÊ®´ó¹¦À;¥ÖÐÉúÎï¼îµÄÑо¿ ¼ÍÐãºì,Åáïΰ,Ìï¾°Ãñ,ÑÖÓñÄý,Àî¼Òʵ Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 42 . (S,P)/(R,M)-4-methoxy-17-nitro-2-oxatricyclo[13.2.2.13,7]-eicosa-1(18),3,5,7(20),15(19),16-hexen-12-ol C20H23NO5 ÏàËÆ¶È:50% The Journal of Organic Chemistry 1999 64 914-924 A Unified Strategy toward the Synthesis of Acerogenin-Type Macrocycles: Total Syntheses of Acerogenins A, B, C, and L and Aceroside IV Gabriela Islas Gonzalez and Jieping Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 43 . isoalstonisine C20H22N2O3 ÏàËÆ¶È:50% Tetrahedron 2000 56 6143-6150 Novel Macroline Oxindoles from a Malayan Alstonia Toh-Seok Kam, Yeun-Mun Choo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 44 . bis-5',5'-nortrachelogenin C40H42O14 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 2012 60 920-923 Four New Dilignans from the Roots of Wikstroemia indica Guo-Cai Wang, Xiao-Li Zhang, Yi-Fei Wang, Guo-Qiang Li, Wen-Cai Ye, Yao-Lan Li Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 45 . Schrenkianaone C20H22O2 ÏàËÆ¶È:50% Chinese Journal of Analytical Chemistry 2009 37 888-892 Elementary Identification of PotentialAutotoxins from Picea Schrenkiana L itters LI Zhao-H u i, WANG Qiang, LIAO Jun-Jun, RUAN X iao, PAN Cun-De, JIANG De-An, LUO Chen-Ca i Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 46 . (R)-2-((2R,3R,4S)-2-(3-Chlorophenyl)-3-nitrochroman-4-yl)cyclohexanone C21H20NO4Cl ÏàËÆ¶È:50% Tetrahedron 2012 68 5810-5816 Synthesis of substituted chiral chromans via organocatalytic kinetic resolution of racemic 3-nitro-2-aryl-2H-chromenes with ketones catalyzed by pyrrolidinyl-camphor-derived organocatalysts Dhananjay R. Magar, Kwunmin Chen Structure 13C NMR ̼Æ×Ä£Äâͼ |

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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 18.2,22.8,35.6,38.3,40.7,50.3,54.0,54.2,58.0,61.5,66.1,69.4,72.1,109.2,112.2,121.7,128.0,128.2,131.9,138.6,140.7,179.4 ÈܼÁÑ¡Ï È«²¿ CDCl3 CD3CD2OD CD2Cl2 C5D5N C3D7NO CD3SOCD3 C4D8O (CH3)4Si C4D8O2 CD3COOD C4D8O2 H2O D2O CF3COOD CD3OD ND3 CD3COCD3 C6D6 CD3CN ²éѯ¿ÕÖµ Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½102¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . gelsemine ÏàËÆ¶È:90.9% Journal of Natural Products 1985 Vol 48 969-971 Studies on the NMR Spectroscopic Properties of Gelsemine--Revisions and Refinements Yeh Schun, Geoffrey A. Cordell Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . gelsemine ÏàËÆ¶È:90.9% Journal of Natural Products 1986 Vol 49 483 21-Oxogelsevirine, a New Alkaloid from Gelsemium rankinii Yeh Schun, Geoffrey A. Cordell, Mark Garland Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . gelsemine ÏàËÆ¶È:90.9% Phytochemistry 1991 30 679-683 Three oxindole alkaloids from Gelsemium species Long-Ze Lin, Schun Yeh, Geoffrey A. Cordell, Chou-Zhou Ni, Jon Clardy Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . Gelsemine ÏàËÆ¶È:86.3% Journal of Asian Natural products Research 2010 12 731-739 Antitumor activity of two gelsemine metabolites in rat liver microsomes Qing-Chun Zhao; Wei Hua; Lin Zhang; Tao Guo; Ming-Hong Zhao; Ming Yan; Guo-Bing Shi; Li-Jun Wu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . gelsemine I C20H22N2O2 ÏàËÆ¶È:81.8% Chinese Traditional and Herbal Drugs 2011 42 222-225 Chemical constituents from Gelsemium elegans ZHANG Zhen, LIU Guang-ming, XIAO Huai, ZHANG Zhen, HE Hong-ping, HAO Xiao-jiang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . Metabolite 1 ÏàËÆ¶È:77.2% Journal of Asian Natural products Research 2010 12 731-739 Antitumor activity of two gelsemine metabolites in rat liver microsomes Qing-Chun Zhao; Wei Hua; Lin Zhang; Tao Guo; Ming-Hong Zhao; Ming Yan; Guo-Bing Shi; Li-Jun Wu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . gelsevirine ÏàËÆ¶È:72.7% Phytochemistry 1991 30 679-683 Three oxindole alkaloids from Gelsemium species Long-Ze Lin, Schun Yeh, Geoffrey A. Cordell, Chou-Zhou Ni, Jon Clardy Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . gelsevirine ÏàËÆ¶È:68.1% Journal of Natural Products 1986 Vol 49 483 21-Oxogelsevirine, a New Alkaloid from Gelsemium rankinii Yeh Schun, Geoffrey A. Cordell, Mark Garland Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . 19-(R)-hydroxydihydrogelsevirine C21H26N2O4 ÏàËÆ¶È:63.6% Phytochemistry 1991 30 679-683 Three oxindole alkaloids from Gelsemium species Long-Ze Lin, Schun Yeh, Geoffrey A. Cordell, Chou-Zhou Ni, Jon Clardy Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . 19-(R)-hydroxydihydrogelsemine C20H24N2O3 ÏàËÆ¶È:63.6% Phytochemistry 1991 30 679-683 Three oxindole alkaloids from Gelsemium species Long-Ze Lin, Schun Yeh, Geoffrey A. Cordell, Chou-Zhou Ni, Jon Clardy Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . corynoxine ÏàËÆ¶È:63.6% Chinese Traditional and Herbal Drugs 1999 30(1) 8-10 ¹³ÌٵĻ¯Ñ§³É·ÖÑо¿(¢ó) ÕÅ¿¢,Ñî³É½ð,Îâ´ó¸Õ Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . methyl (2R,3aR,5aS,6S,9aS,9bS)-2-(3-furyl)-6,9a-dimethyl-3a-methylaminoperhydronaphtho-[2,1-b]furan-6-carboxylate [methyl 8¦Á,12¦Á : 15,16-diepoxy-17-methylaminolabda-13(16),14-dien-18-oate] C22H33NO4 ÏàËÆ¶È:63.6% Russian Journal of Organic Chemistry 2005 41 535-545 Synthetic Transformations of Higher Terpenoids: IX. Nitrogen-Containing Heterocyclic Compounds on the Basis of Lambertianic Acid S. V. Chernov, E. E. Shul¡¯ts, M. M. Shakirov, I. Yu. Bagryanskaya and Yu. V. Gatilov, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . 18,19-dehydrocorynoxinic acid C21H24N2O4 ÏàËÆ¶È:59.0% Journal of Natural Products 2008 71(7) 1271-1274 Alkaloids from the Leaves of Uncaria rhynchophylla and Their Inhibitory Activity on NO Production in Lipopolysaccharide-Activated Microglia Dan Yuan, Bin Ma, Chunfu Wu, Jingyu Yang, Lijia Zhang, Suiku Liu, Lijun Wu, and Yoshihiro Kano Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . (R,pS)-5-{N-methyl-1-[2-diphenylphosphanyl)ferrocenyl]ethylamino}valeric acid C30H34O2NPFe ÏàËÆ¶È:59.0% Molecules 2005 10 679-692 Immobilization of Chiral Ferrocenyl Ligands on Silica Gel and their Testing in Pd-catalyzed Allylic Substitution and Rh-catalyzed Hydrogenation J¨¢n Cvengroš, Štefan Toma, M¨¢ria Žemb¨¦ryov¨¢ and Duncan J. Macquarrie Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . kopsiloscine A C23H26N2O6 ÏàËÆ¶È:56.5% Journal of Natural Products 2007 70 1783-1789 Biologically Active Aspidofractinine, Rhazinilam, Akuammiline, and Vincorine Alkaloids from Kopsia G. Subramaniam, Osamu Hiraku,Masahiko Hayashi, Takashi Koyano, Kanki Komiyama, and Toh-Seok Kam Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . (2R,3R,12bS)-2-[2-(Benzyloxy)ethyl]-7a-chloro-1,2,3,4,6,7,7a,12boctahydroindolo[2,3-a]quinolizine-3-carbaldehyde C25H27ClN2O2 ÏàËÆ¶È:56.5% European Journal of Organic Chemistry 2012 398-408 Concise Total Synthesis of Dihydrocorynanthenol, Protoemetinol, Protoemetine, 3-epi-Protoemetinol and Emetine Shuangzheng Lin, Luca Deiana, Abrehet Tseggai and Armando C¨®rdova Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . yohimbine ÏàËÆ¶È:54.5% Journal of Natural Products 2001 64 193-195 Hydroxylation of Yohimbine in Superacidic Media: One-Step Access to Human Metabolites 10 and 11-Hydroxyyohimbine Alain Duflos,Florence Redoules,Jacques Fahy, Jean-Claude Jacquesy, and Marie-Paule Jouannetaud Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . Kopsinginol C19H22N2O ÏàËÆ¶È:54.5% Phytochemistry 1996 42 539-541 Three aspidofractinine-type alkaloids from Kopsia teoi Toh-Seok Kam, K. Yoganathan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . 21-oxogelsemine ÏàËÆ¶È:54.5% Journal of Natural Products 1986 Vol 49 483 21-Oxogelsevirine, a New Alkaloid from Gelsemium rankinii Yeh Schun, Geoffrey A. Cordell, Mark Garland Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . 19-(S)-hydroxydihydroxygelsevirine ÏàËÆ¶È:54.5% Phytochemistry 1991 30 679-683 Three oxindole alkaloids from Gelsemium species Long-Ze Lin, Schun Yeh, Geoffrey A. Cordell, Chou-Zhou Ni, Jon Clardy Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . (6aS*,8S*,11aR*)-7-Benzyl-6a,7,8,9,10,11-hexahydro-6H-8,11a-methanochromeno[3,4-b]azepin-4-ol C21H23NO2 ÏàËÆ¶È:54.5% Bioorganic & Medicinal Chemistry 2011 19 3434-3443 Probes for narcotic receptor mediated phenomena. Part 42: Synthesis and in vitro pharmacological characterization of the N-methyl and N-phenethyl analogues of the racemic ortho-c and para-c oxide-bridged phenylmorphans Jin-Hee Kim, Jeffrey R. Deschamps,Richard B. Rothman, Christina M. Dersch, John E. Folk ,Kejun Cheng, Arthur E. Jacobson, Kenner C. Rice Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . 4-(2-Ethoxyethoxymethyl)-N-[3-[4-(2-methoxyphenyl)-piperazin-1-yl]propyl] benzamide C26H37N3O4 ÏàËÆ¶È:54.5% Bioorganic & Medicinal Chemistry 2012 20 455-466 Bivalent molecular probes for dopamine D2-like receptors Daniela Huber, Stefan Löber, Harald H¨¹bner, Peter Gmeiner Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . compound 10 C21H26N2O4 ÏàËÆ¶È:54.5% Chemical & Pharmaceutical Bulletin 1987 35 4668-4671 INDOLE ALKALOIDS ISOLATED FROM GELSEMIUM ELEGANS (THAILAND) : 19- (Z) -AKUAMMIDINE, 16-EPI-VOACARPINE, 19-HYDROXYDIHYDRO-GELSEVIRINE, AND THE REVISED STRUCTURE OF KOUMIDINE Shin-ichiro Sakai,Sumphan Wongseripipatana,Dhavadee Ponglux,Masaki Yokota,Koreharu Ogata,Hiromitsu Takayama and Norio Aimi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . corynoxeine ÏàËÆ¶È:54.5% Chinese Journal of Medicinal Chemistry 2006 16 369-372 Chemical constituents of the leaves of Uncaria rhynchophylla (Miq.) Jacks. WANG Bing, YUAN Dan, MA Bin, XIE Yuan-yuan, YIN Jun, KANO Yoshihiro Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 25 . isorhynchophylline ÏàËÆ¶È:54.5% Chinese Journal of Medicinal Chemistry 2006 16 369-372 Chemical constituents of the leaves of Uncaria rhynchophylla (Miq.) Jacks. WANG Bing, YUAN Dan, MA Bin, XIE Yuan-yuan, YIN Jun, KANO Yoshihiro Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 26 . neocarazostatin B C22H27NO3 ÏàËÆ¶È:54.5% The Journal of Antibiotics 1991 44 903-907 STUDIES ON FREE RADICAL SCAVENGING SUBSTANCES FROM MICROORGANISMS II. NEOCARAZOSTATINS A, B AND C, NOVEL FREE RADICAL SCAVENGERS SHINICHIRO KATO, KAZUTOSHI SHINDO, YOKO KATAOKA, YUJI YAMAGISHI, JUNICHIRO MOCHIZUKI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 27 . compound 10 ÏàËÆ¶È:54.5% Chinese Chemical Letters 2011 22 781-784 Synthesis and biological evaluation of andrographolide derivatives as potent anti-HIV agents Bin Wang, Jing Li, Wen Long Huang, Hui Bin Zhang, Hai Qian, Yong Tang Zheng Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 28 . 3-[(2S,3R,4R,5S,6S)-2-Benzyloxymethyl-5-(tert-butyldimethylsilyloxy)-6-methoxy-3-pivaloyloxymethyltetr-ahydropyran-4-yl]propyl pivalate C34H58O8Si ÏàËÆ¶È:54.1% Bioorganic & Medicinal Chemistry 2008 16 3002-3024 The 2¦Á-(3-hydroxypropyl) group as an active motif in vitamin D3 analogues as agonists of the mutant vitamin D receptor (Arg274Leu) Shinobu Honzawa, Yasuhiro Yamamoto, Atsushi Yamashita, Takayuki Sugiura, Masaaki Kurihara, Midori A. Arai, Shigeaki Kato, Atsushi Kittaka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 29 . kopsiloscine C C23H28N2O7 ÏàËÆ¶È:52.1% Journal of Natural Products 2007 70 1783-1789 Biologically Active Aspidofractinine, Rhazinilam, Akuammiline, and Vincorine Alkaloids from Kopsia G. Subramaniam, Osamu Hiraku,Masahiko Hayashi, Takashi Koyano, Kanki Komiyama, and Toh-Seok Kam Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 30 . 3S-ethoxy-19-epi-heyneanine C23H30N2O4 ÏàËÆ¶È:52.1% Journal of Natural Products 2002 65 669-672 Five New Iboga Alkaloids from Tabernaemontana corymbosa Toh-Seok Kam and Kooi-Mow Sim Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 31 . methyl (19¦Á,20¦Á)-14,16-didehydro-1-hydromehtyl-14-methylene oxayohimban-16-carboxylate ÏàËÆ¶È:52.1% Journal of Natural Products 1985 Vol 48 273-278 Partial Synthesis via Indole Alkaloids: A New Hexacyclic Derivative of (-)-Tetrahydroalstonine Bernhard Mompon, Thierry Vassal, Philippe Poirier Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 32 . N-carbomethoxy-17¦Â-hydroxy-∆-14,15-kopsinine ÏàËÆ¶È:52.1% Journal of Natural Products 1988 Vol 51 703 Nouveaux Alcaloïdes de Type Aspidofractinine Fonctionnalises en C-17, Extraits des Écorces de Tronc d'un Kopsia de Malaisie C. Kan-Fan, S. K. Kan, J. R. Deverre, J. C. Quirion, H. P. Husson, Y. L. Zhou, K. C. Chan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 33 . 2(S)-2-methyl-2-(4-methyl-3-pentenyl)-7-hydroxy-5-(2-phenylethyl)chromene monomethyl ether C25H30O2 ÏàËÆ¶È:52.1% Phytochemistry 1991 30 219-234 Prenyl bibenzyls from the liverwort Radula kojana Yoshinori Asakawa, Keiko Kondo, N¨¦e K. Takikawa, Motoo Tori, Toshihiro Hashimoto, Shunichi Ogawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 34 . 19-(R)-acetyldihydrogelsevirine C23H28N2O5 ÏàËÆ¶È:52.1% Phytochemistry 1991 30 679-683 Three oxindole alkaloids from Gelsemium species Long-Ze Lin, Schun Yeh, Geoffrey A. Cordell, Chou-Zhou Ni, Jon Clardy Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 35 . 4-(2-Ethoxyethoxymethyl)-N-[4-[4-(2-methoxyphenyl)-piperazin-1-yl]butyl] benzamide C27H39N3O4 ÏàËÆ¶È:52.1% Bioorganic & Medicinal Chemistry 2012 20 455-466 Bivalent molecular probes for dopamine D2-like receptors Daniela Huber, Stefan Löber, Harald H¨¹bner, Peter Gmeiner Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 36 . 3-benzyl-4-(2-hydroxyethyl)-2,3,3a,4,5,7-hexahydro-1H-pyrrolo[2,3-d]carbazole-6-carboxylic acid methyl ester C25H28N2O3 ÏàËÆ¶È:52.1% Heterocycles 2006 68 2301-2317 Synthesis of Vinca Alkaloids and Related Compounds. Part 106. An Efficient Convergent Synthetic Pathway to Build Up the Ibophyllidine Skeleton II. Total Synthesis of (¡À)-Deethylibophyllidine and (¡À)-14-Epi-deethylibophyllidine Fl¨®ri¨¢n T¨®th, György Kalaus,* Istv¨¢n Greiner, M¨¢ria Kajt¨¢r-Peredy, Ágnes Gömöry, L¨¢szl¨® Hazai, and Csaba Sz¨¢ntay* Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 37 . S-D-Biotinoyl-4-aminobenzyl 5-acetamido-3,5-dideoxy-2-thio-D-glycero-¦Á-D-galacto-2-nonulopyranosidonic acid C28H41N4O10S2 ÏàËÆ¶È:52.1% Bioorganic & Medicinal Chemistry 2000 8 2709-2718 The synthesis of biotinylated carbohydrates as probes for carbohydrate-recognizing proteins Donald I Angus, Milton J Kiefel, Mark von Itzstein Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 38 . sibanomicin ÏàËÆ¶È:52.1% The Journal of Antibiotics 1988 41 1281-1284 SIBANOMICIN, A NEW PYRROLO[1, 4]- BENZODIAZEPINE ANTITUMOR ANTIBIOTIC PRODUCED BY A MICROMONOSPORA SP. JIRO ITOH, HIRO-OMI WATABE, SHIGETAKA ISHII, SHUICHI GOMI, MIEKO NAGASAWA, HARUO YAMAMOTO, TAKASHI SHOMURA, MASAJI SEZAKI, SHINICHI KONDO Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 39 . 2'-(1-Morpholinyl)-ethyl (3S,16R)-apovincaminate¡¤2 tartaric acid C35H45O15N3 ÏàËÆ¶È:52% Chinese Journal of Natural Medicines 2011 9 51-57 Synthesis of Novel Alkylamino Substituted cis and trans Apovincamate Derivatives SHENG Hua-Ming, XIANG Zuo-Juan, YE Jun-Ting, ZHENG Jin-Hong *, SUN Hong-Bin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 40 . 12-hydroxy-11-methoxyhenningsamine ÏàËÆ¶È:50% Chemistry & Biodiversity 2008 Vol. 5 1345 A New Indole Alkaloid and Anti-Inflammatory Constituents from Strychnos cathayensis Jih-Jung Chen, Yu-Ting Luo, Tsong-Long Hwang, Ping-Jyun Sung, Tai-Chi Wang, Ih-Sheng Chen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 41 . 9-deacetylfumigaclavine C C21H28N2O ÏàËÆ¶È:50% Journal of Natural Products 2009 72 753-755 Bioactive Alkaloids from Endophytic Aspergillus fumigatus Hui Ming Ge, Zhi Guo Yu, Jie Zhang, Jun Hua Wu, and Ren Xiang Tan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 42 . kopsiloscine H C21H24N2O4 ÏàËÆ¶È:50% Journal of Natural Products 2008 71(1) 53-57 Biologically Active Aspidofractinine Alkaloids from Kopsia singapurensis G. Subramaniam, Osamu Hiraku, Masahiko Hayashi, Takashi Koyano, Kanki Komiyama, and Toh-Seok Kam Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 43 . cleospinol B C20H32O3 ÏàËÆ¶È:50% Journal of Natural Products 2004 67 179-183 New Cembranes from Cleome spinosa Dwight O. Collins, William F. Reynolds, and Paul B. Reese Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 44 . cephalotaxine ¦Á-N-oxide C18H21NO5 ÏàËÆ¶È:50% Journal of Natural Products 2003 66 152-154 New Alkaloids from Cephalotaxus fortunei Mamadou Bocar, Akino Jossang, and Bernard Bodo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 45 . 11-hydroxyyohimbine C21H26N2O4 ÏàËÆ¶È:50% Journal of Natural Products 2001 64 193-195 Hydroxylation of Yohimbine in Superacidic Media: One-Step Access to Human Metabolites 10 and 11-Hydroxyyohimbine Alain Duflos,Florence Redoules,Jacques Fahy, Jean-Claude Jacquesy, and Marie-Paule Jouannetaud Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 46 . compound 4 ÏàËÆ¶È:50% Journal of Natural Products 1996 59 880-882 8-Hydroxysalviarin and 7, 8-Didehydrorhyacophiline, Two New Diterpenes from Salvia reflexa Matias Nieto, Oscar Gallardo V., Pedro C. Rossomando, and Carlos E. Tonn Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 47 . Nb-demethylechitamine N-oxide C21H26N2O5 ÏàËÆ¶È:50% Planta Medica 1988 54 480-481 Nb-Demethylechitamine N-Oxide from Roots of Winchia calophylla Chen Wei Ming, Zhang Pei Ling, and U. R¨¹cker Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 48 . malindine C20H21N3 ÏàËÆ¶È:50% Planta Medica 1981 43 353-359 Quaternary Indole Alkaloids of Strychnos decussata Ajibola A. Olaniyi, Wenche N. A. Rolfsen and Rob Verpoorte Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 49 . sakerinol B C22H31NO6S ÏàËÆ¶È:50% Phytochemistry 2000 54 207-213 Prenylated sulfonyl amides from Glycosmis species Otmar Hofer, Harald Greger, Brigitte Lukaseder, Srunya Vajrodaya, Markus Bacher Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 50 . uncarine E ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 1993 41 2077-2086 A Nuclear Magnetic Resonance Study on the Eleven Stereoisomers of Heteroyohimbine-Type Oxindole Alkaloids Hiroko SEKI,Hiromitsu TAKAYAMA,Norio AIMI,Shin-ichiro SAKAI and Dhavadee PONGLUX Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 51 . uncarine C ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 1993 41 2077-2086 A Nuclear Magnetic Resonance Study on the Eleven Stereoisomers of Heteroyohimbine-Type Oxindole Alkaloids Hiroko SEKI,Hiromitsu TAKAYAMA,Norio AIMI,Shin-ichiro SAKAI and Dhavadee PONGLUX Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 52 . drevogenin D ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 1985 33 2287-2293 Studies on the Constituents of Asclepiadaceae Plants. LIX. The Structures of Five New Glycosides from Dregea volubilis (L.) BENTH. SHINICHI YOSHIMURA,HIROMI NARITA,KOJI HAYASHI and HIROSHI MITSUHASHI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 53 . malagashanol C22H30N2O3 ÏàËÆ¶È:50% Phytochemistry 1999 51 479-486 Minor Nb,C(21)-secocuran alkaloids of Strychnos myrtoides Marie-Therese Martin, Philippe Rasoanaivo, Giovanna Palazzino, Corrado Galeffi, Marcello Nicoletti, Francois Trigalo, Francois Frappier Structure 13C NMR ̼Æ×Ä£Äâͼ |

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